The Molecular Basis of Alcohol's Actions

酒精作用的分子基础

• 批准号: 7929877
• 负责人: DAVID NIGEL JONES
• 金额: $ 38.25万
• 依托单位: UNIVERSITY OF COLORADO DENVER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-25 至 2012-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7929877
• 关键词: Affect; Affinity; Alcoholism; Alcohols; Amino Acid Substitution; Amino Acids; Binding; Binding Sites; Biochemical; Biological Assay; Chemicals; DAG/PE-Binding Domain; Data; Development; Drosophila inturned protein; Drosophila odorant binding protein; Enzymes; Ethanol; Exhibits; Family; Funding; Future; Genetic Markers; Glycine Receptors; Goals; Health; Human; Hydrogen Bonding; Ion Channel; Knowledge; Lead; Length; Methods; Modeling; Molecular; Mutation; NMR Spectroscopy; Nature; Neuraxis; Pharmaceutical Preparations; Play; Predisposition; Protein Kinase C; Protein Kinase C Alpha; Proteins; Relative (related person); Sampling; Signaling Molecule; Site; Specificity; Structure; Testing; Transmembrane Domain; Work; addiction; alcohol response; alcohol sensitivity; base; citrate carrier; cofactor; enzyme activity; insight; novel strategies; novel therapeutic intervention; phosphatidylethanol; prevent; protein structure function; public health relevance; receptor; receptor function; structural biology

DESCRIPTION (provided by applicant): The long term goal of this project is to understand the molecular mechanisms of alcohol's actions. Due to its small size and lack of chemical features, alcohol is often considered to be a relatively non-specific drug. Many cellular factors have been identified that contribute to regulating cellular responses to ethanol that ultimately lead to the development of addiction. However, it is clear that alcohol does not interact with all these proteins, but in fact shows a relatively high degree of specificity for a limited number of receptors, ion channels and other signaling molecules. This led to the hypothesis that in many cases alcohol acts by binding to specific sites in these proteins to bring about changes in protein structure and function. However, there is very little knowledge about what makes up an alcohol binding site and contribute to alcohol sensitivity. Previously, we identified a specific alcohol binding site in the Drosophila protein LUSH. Structural and biochemical studies of this protein led to the discovery that concerted interactions from multiple hydrogen bonding resides were required to form an ethanol binding site. In this work we will focus on determining the interactions between alcohol and regulatory domains of Protein Kinase C (PKC) family of enzymes. Several isoforms of PKC proteins play a central in regulating responses to ethanol. Further, several isoforms of PKC have been shown to be directly sensitive to alcohol and it is suggested that ethanol can modulate binding of important cofactors required for sub-cellular localization and activation. We will use structural biology methods to determine how alcohol interacts with these domains, and how these interactions lead to changes in structure and dynamics that could alter the ability of PKC domains to interact with co-factors. We have already collected preliminary data that have identified a specific interaction between alcohol and PKC-alpha. Finally we propose to investigate the interactions between alcohol and the transmembrane domains of the glycine receptor. Glycine receptors are one of the primary targets of alcohol in the central nervous systems, and a wealth of studies have developed a model for how alcohol may affect the function of this receptor. Our studies will determine what residues are critical for binding alcohol, an how the known mutations are likely to its modify alcohol sensitivity PUBLIC HEALTH RELEVANCE Understanding how ethanol acts to modulate protein structure and function is a fundamental problem relevant to human health. Defining the sites of alcohol actions in proteins, and how amino acids in these sites contribute to ethanol sensitivity, will provide a greater understanding of the mechanism of alcohol's actions. This may allow future development of novel approaches to prevent alcohols actions, and the identification of genetic markers associated with a predisposition to alcoholism.

描述（由申请人提供）：该项目的长期目标是了解酒精作用的分子机制。由于其体积小，缺乏化学特征，酒精通常被认为是一种相对非特异性的药物。许多细胞因子已被确定，有助于调节细胞对乙醇的反应，最终导致成瘾的发展。然而，很明显，酒精并不与所有这些蛋白质相互作用，但实际上对有限数量的受体、离子通道和其他信号分子显示出相对较高的特异性。这导致了一种假设，即在许多情况下，酒精通过与这些蛋白质中的特定位点结合来改变蛋白质结构和功能。然而，关于酒精结合位点的组成和对酒精敏感性的贡献知之甚少。以前，我们确定了一个特定的酒精结合位点的果蝇蛋白LUSH。这种蛋白质的结构和生物化学研究导致发现，从多个氢键残基的协同相互作用，需要形成一个乙醇结合位点。在这项工作中，我们将集中在确定酒精和蛋白激酶C（PKC）家族的酶的调节结构域之间的相互作用。PKC蛋白的几种亚型在调节乙醇反应中起着重要作用。此外，PKC的几种亚型已被证明是直接敏感的酒精，它表明，乙醇可以调节亚细胞定位和激活所需的重要辅因子的结合。我们将使用结构生物学方法来确定酒精如何与这些结构域相互作用，以及这些相互作用如何导致结构和动力学的变化，从而改变PKC结构域与辅因子相互作用的能力。我们已经收集了初步数据，确定了酒精和PKC-α之间的特定相互作用。最后，我们建议研究乙醇和甘氨酸受体的跨膜结构域之间的相互作用。甘氨酸受体是酒精在中枢神经系统中的主要靶点之一，大量的研究已经建立了酒精如何影响这种受体功能的模型。我们的研究将确定哪些残基对结合酒精至关重要，以及已知的突变如何可能改变酒精敏感性公共卫生相关性了解乙醇如何调节蛋白质结构和功能是与人类健康相关的基本问题。确定蛋白质中酒精作用的位点，以及这些位点中的氨基酸如何对酒精敏感性做出贡献，将有助于更好地理解酒精作用的机制。这可能使未来开发新的方法来防止酒精的行动，并确定与酗酒倾向相关的遗传标记。